Literature DB >> 12767824

A less laborious approach to the high-throughput production of recombinant proteins in Escherichia coli using 2-liter plastic bottles.

Cynthia Sanville Millard1, Lucy Stols, Pearl Quartey, Youngchang Kim, Irina Dementieva, Mark I Donnelly.   

Abstract

Contemporary approaches to biology often call for the high-throughput production of large amounts of numerous proteins for structural or functional studies. Even with the highly efficient protein expression systems developed in Escherichia coli, production of these proteins is laborious and time-consuming. We have simplified established protocols by the use of disposable culture vessels: common 2-liter polyethylene terephthalate beverage bottles. The bottles are inexpensive, fit conveniently in commonly available flask holders, and, because they are notched, provide sufficient aeration to support the growth of high-density cultures. The use of antibiotics and freshly prepared media alleviates the need for sterilization of media and significantly reduces the labor involved. Uninoculated controls exhibited no growth during the time required for protein expression in experimental cultures. The yield, solubility, activity, and pattern of crystallization of proteins expressed in bottles were comparable to those obtained under conventional culture conditions. After use, the bottles are discarded, reducing the risk of cross-contamination of subsequent cultures. The approach appears to be suitable for high-throughput production of proteins for structural or functional studies.

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Year:  2003        PMID: 12767824     DOI: 10.1016/s1046-5928(03)00063-9

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  26 in total

1.  Automation of protein purification for structural genomics.

Authors:  Youngchang Kim; Irina Dementieva; Min Zhou; Ruiying Wu; Lour Lezondra; Pearl Quartey; Grazyna Joachimiak; Olga Korolev; Hui Li; Andrzej Joachimiak
Journal:  J Struct Funct Genomics       Date:  2004

2.  Economical parallel protein expression screening and scale-up in Escherichia coli.

Authors:  Oleg Brodsky; Ciarán N Cronin
Journal:  J Struct Funct Genomics       Date:  2006-12-23

3.  Enhanced bacterial protein expression during auto-induction obtained by alteration of lac repressor dosage and medium composition.

Authors:  Paul G Blommel; Katie J Becker; Petar Duvnjak; Brian G Fox
Journal:  Biotechnol Prog       Date:  2007-05-17

Review 4.  High-throughput protein purification and quality assessment for crystallization.

Authors:  Youngchang Kim; Gyorgy Babnigg; Robert Jedrzejczak; William H Eschenfeldt; Hui Li; Natalia Maltseva; Catherine Hatzos-Skintges; Minyi Gu; Magdalena Makowska-Grzyska; Ruiying Wu; Hao An; Gekleng Chhor; Andrzej Joachimiak
Journal:  Methods       Date:  2011-08-31       Impact factor: 3.608

5.  Broad-substrate screen as a tool to identify substrates for bacterial Gcn5-related N-acetyltransferases with unknown substrate specificity.

Authors:  Misty L Kuhn; Karolina A Majorek; Wladek Minor; Wayne F Anderson
Journal:  Protein Sci       Date:  2012-12-17       Impact factor: 6.725

6.  A novel polyamine allosteric site of SpeG from Vibrio cholerae is revealed by its dodecameric structure.

Authors:  Ekaterina V Filippova; Misty L Kuhn; Jerzy Osipiuk; Olga Kiryukhina; Andrzej Joachimiak; Miguel A Ballicora; Wayne F Anderson
Journal:  J Mol Biol       Date:  2015-01-23       Impact factor: 5.469

7.  Crystal structure of a type II dehydroquinate dehydratase-like protein from Bifidobacterium longum.

Authors:  Samuel H Light; Sankar N Krishna; Raymond C Bergan; Arnon Lavie; Wayne F Anderson
Journal:  J Struct Funct Genomics       Date:  2013-03-29

8.  Structure and protective efficacy of the Staphylococcus aureus autocleaving protease EpiP.

Authors:  Misty L Kuhn; Prachi Prachi; George Minasov; Ludmilla Shuvalova; Jiapeng Ruan; Ievgeniia Dubrovska; James Winsor; Monica Giraldi; Massimiliano Biagini; Sabrina Liberatori; Silvana Savino; Fabio Bagnoli; Wayne F Anderson; Guido Grandi
Journal:  FASEB J       Date:  2014-01-13       Impact factor: 5.191

9.  Production of selenomethionine-labeled proteins in two-liter plastic bottles for structure determination.

Authors:  Lucy Stols; Cynthia Sanville Millard; Irina Dementieva; Mark I Donnelly
Journal:  J Struct Funct Genomics       Date:  2004

10.  Production in two-liter beverage bottles of proteins for NMR structure determination labeled with either 15N- or 13C-15N.

Authors:  Qin Zhao; Ronnie Frederick; Kory Seder; Sandy Thao; Hassan Sreenath; Francis Peterson; Brian F Volkman; John L Markley; Brian G Fox
Journal:  J Struct Funct Genomics       Date:  2004
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